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Pyrido[3,4-e][1,2,4]triazine is a heterocyclic compound characterized by a fused ring structure consisting of a pyridine ring attached to a [1,2,4]triazine ring. This chemical structure is notable for its potential applications in various fields, including pharmaceuticals and materials science, where it may be used as a building block for the synthesis of more complex molecules. The compound's unique electronic properties and stability make it an interesting target for chemical research and development.

767-95-3

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767-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 767-95-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 767-95:
(5*7)+(4*6)+(3*7)+(2*9)+(1*5)=103
103 % 10 = 3
So 767-95-3 is a valid CAS Registry Number.

767-95-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrido[3,4-e][1,2,4]triazine

1.2 Other means of identification

Product number -
Other names pyrido<3,4-e>as-triazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:767-95-3 SDS

767-95-3Downstream Products

767-95-3Relevant academic research and scientific papers

Pyrido[3,4-e]-1,2,4-triazines and related heterocycles as potential antifungal agents

Reich,Fabio,Lee,Kuck,Testa

, p. 2474 - 2485 (2007/10/02)

The preparation and biological activities of a series of pyrido[3,4-e]-1,2,4-triazines, 1,2,4-triazino[5,6-c]quinolines, and related fused triazines are described. Methyl, amino, and acylamino substituents were placed in the pyridyl ring of the former system. Other structural modifications included various alkyl, cycloalkyl, substituted phenyl, and heterocyclic groups in the 3-position of these ring systems. In agar dilution assays, actives in this series inhibited strains of Candida, Aspergillus, Mucor, and Trychophyton species at MIC's of ≤ 16 μg/mL.

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